Fluorescent Affinity Tag to Enhance Phosphoprotein Detection and Characterization

ABSTRACT

The invention relates to target-associative tags incorporating cysteamine as the target-associative moiety. The invention further relates to a method for producing a target-associative tag by addition of cysteamine as the target-associative moiety to another molecule or entity having a property or properties useful in discriminating or selecting between members of a set, where such properties could include, for example, fluorescence, mass, affinity, reactivity, size, absorbance, magnetism, subatomic spin characteristics, or an ability to associate specifically or preferentially with certain structures. The invention further relates to a method for analyzing, identifying, or purifying phosphorylated proteins or phosphorylated protein fragments using a tag having the properties of both fluorescence and affinity.

FIELD OF THE INVENTION

The invention relates to target-associative tags incorporating cysteamine as the target-associative moiety. The invention further relates to a method for producing a target-associative tag by addition of cysteamine as the target-associative moiety to another molecule or entity having a property or properties useful in discriminating or selecting between members of a set, where such properties could include, for example, fluorescence, mass, affinity, reactivity, size, absorbance, magnetism, subatomic spin characteristics, or an ability to associate specifically or preferentially with certain structures. The invention further relates to a method for analyzing, identifying, or purifying phosphorylated proteins or phosphorylated protein fragments using a tag having the properties of both fluorescence and affinity.

BACKGROUND OF THE INVENTION

The subject invention relates to the art of preparing target-associative tags. Such tags are widely used in science, medicine, and elsewhere for a variety of purposes including as aids to visualization or purification. Typically, such tags comprise both a moiety having an ability to associate specifically or preferentially with certain structures [“targeting moiety”] and a moiety having a property or properties useful in discriminating or selecting between members of a set [“discriminating moiety”].

When a target-associative tag associates with its target, a tag-target conjugate is formed. In forming such a tag-target conjugate, the target typically acquires the useful property or properties of the tag. For example, an antibody-associative fluorescent tag can be associated with an antibody to confer the property of fluorescence upon the antibody. The association of the tag and the target in the tag-target conjugate can be based on the formation of one or more covalent bonds, an affinity interaction, a hydrophobic interaction, a hydrogen-bonding interaction, a magnetic interaction, or any other type of interaction that imparts an ability to associate specifically or preferentially with certain structures.

A tag-target conjugate may itself function as a target-associative tag in some cases. For example, when an antibody is tagged with a fluorophore to produce a fluorescent antibody, the fluorescent antibody can then be regarded as target-associative tag that may be directed against structures to which the antibody has an affinity.

There are a wide variety of properties that may be useful in a target-associative tag. In general, any property or properties useful in discriminating or selecting between members of a set could have utility in a target-associative tag. Such properties include, but are not limited to, fluorescence, mass, affinity, reactivity, size, absorbance, magnetism, subatomic spin characteristics, or an ability to associate specifically or preferentially with certain structures.

Practitioners skilled in the art will recognize that although target-associative tags have been described here as often comprising both a targeting moiety and a discriminating moiety, in some cases the classification of a given moiety as a targeting moiety or a discriminating moiety may be ambiguous or subject to context. For instance, a rhodamine moiety incorporated into a target-associative tag might often be regarded as a discriminating moiety in that it may exhibit fluorescence under certain conditions, but the same rhodamine moiety might also be regarded as a targeting moiety in that it may exhibit an affinity interaction with certain structures. In general, the set of all possible targeting moieties is a subset of the set of all possible discriminating moieties; every targeting moiety by definition has a property or properties useful in discriminating or selecting between members of a set in that every targeting moiety is able to specifically or preferentially associate with certain structures. In other words, every targeting moiety is also a discriminating moiety, but there may be discriminating moieties that are not targeting moieties.

While target-associative tags typically comprise both a targeting moiety and a discriminating moiety, it is possible that a single moiety could fulfill both roles. For example, in certain fluorogenic reagents known in the art it might be difficult, impossible, or simply of little descriptive utility to identify separate targeting and discriminating moieties. For example, 7-N,N-dimethylsulfonyl-4-(2,1,3-benzoxadiazolyl)isothiocyanate, also known as DBD-NCS, is a fluorogenic reagent used in peptide sequencing analysis. In associating with its target via the formation of a covalent bond, DBD-NCS is converted from a fluorogenic form to a fluorescent form. Thus the target-reactive moiety is a component of the fluorogenic/fluorescent moiety. Also, just as it is possible that a single moiety could fulfill the roles of both discriminating moiety and targeting moiety, it is also possible that a target-associative tag could contain multiple discriminating moieties or multiple targeting moieties or both.

One way of discriminating between members of a set is by fluorescent emission. For instance, the set of all structures within a cell can be differentiated by degree of fluorescence when visualizing the cell. Fluorescent target-associative tags are widely used for this purpose. For example, phalloidin is a cyclic peptide produced by the poisonous mushroom, Amanita phalloides. Conjugation of phalloidin as the targeting moiety and the fluorophore rhodamine as the discriminating moiety produces a target-associative tag that associates preferentially with actin bundles, allowing visualization of said actin bundles by fluorescence microscopy. Another common type of fluorescent target-associative tag is formed by conjugation of a fluorophore and an antibody. Such a fluorescent target-associative tag can be directed against structures to which the antibody has an affinity. For example, a target-associative tag consisting of the fluorophore Texas Red conjugated with a goat anti-mouse immunoglobulin can be directed against mouse primary antibodies for the purpose of visualizing cell structures.

Historically, initial difficulties in establishing the localization of phosphorylated residues in proteins led to the development of a scheme by which phosphoserine and phosphothreonine residues were modified by beta-elimination followed by nucleophilic attack to give a derivatized residue. Such a scheme has been known in the art for at least 32 years. [Simpson, D. L. et al., Biochemistry 111:1849-1856, 1972; Kolesnikova, V. Y. et al., Biokhimiya 39:235-240 (Engl. Trans.) 1974]. Subsequent refinement of the technique has frequently favored thiols as the preferred nucleophile, and the use of thiols as nucleophiles in the scheme has been known in the art for at least 25 years. [Clark, R. C. and Dijkstra, J., Int. J. Biochem. 11:577-585, 1979].

Many modifications of the beta-elimination/nucleophilic attack technique are known in the art, and such modifications frequently involve the use of target-associative tags as nucleophiles to imbue the derivatized phosphoresidues with a desired property. One type of modification incorporates fluorophores. Use of pyridoxamine and fluorescence detection allows detection of low picomolar quantities of a phosphorylated polypeptide. [Hastings, T. G. and Reimann E. M, FEB 231(2):431-436, 1988]. Use of fluorescein and laser-induced fluorescence allows detection of attomolar quantities of phosphoserine-containing peptides and proteins. [Fadden, P. and Haystead, T. A., Anal. Biochem. 225(1):81-88, 1995].

Another type of modification incorporates an affinity tag. Beta-elimination and subsequent nucleophilic attack by ethanedithiol, followed by addition of biotin to the resulting free thiol group, allows for affinity isolation and enrichment of protein fragments containing phosphorylated residues. [Adamczyk, M. et al., Rapid Comm. Mass. Spec. 15:1481-1488, 2001; Oda, Y. et al., Nature Biotechnol. 19:379-382, 2001]. A further refinement that utilizes nucleophilic attack by a tag containing both biotin and isotopic mass markers may be particularly useful for mass spectroscopy following affinity purification. [Goshe, M. B. et al., Anal. Chem. 73:2578-2586, 2001; Goshe, M. B. et al., Anal. Chem. 74:607-616, 2001]. An introduced thiol tag can also be used directly for affinity purification on an activated thiol resin. [McLachlin, D. T. and Chait, B. T., Anal. Chem. 75(24):6826-6836, 2003].

Target-associative tags that mimic lysine have been used in the beta-elimination/Michael addition scheme to introduce additional enzyme-mediated proteolysis sites at phosphoserine and phosphothreonine residues, thus facilitating the analysis of proteins containing such residues. [Knight, Z. A. et al., Nature Biotechnol. 21(9):1047-1054, 2003].

BRIEF SUMMARY OF THE INVENTION

The present invention pertains to methods and compositions suitable for facilitating the analysis, identification, or purification of thiol-reactive molecules. In one embodiment, the invention relates to analysis, identification, or purification of phosphoproteins. Phosphoproteins or fragments thereof may often be present in small amounts as part of complex mixtures. Incorporation of a fluorescent affinity tag (FAT) at phosphorylated residues permits both enhanced detection and facile purification with minimal sample manipulation.

In another embodiment, the invention relates the preparation of target-associative tags containing a thiol moiety. Many fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties can be usefully employed in a variety of scenarios dependent on covalent attachment of said discriminating moieties to a reactive thiol (such as a cysteamine) capable of acting as a targeting moiety. The reaction of cysteamine or cysteamine-derivatives with said discriminating moieties provides a useful way of preparing such target-associative tags.

BRIEF DESCRIPTION OF THE FIGURES

FIG. 1 depicts a matrix assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrum showing reaction efficiency after beta elimination of a high performance liquid chromatography (HPLC)-purified monophoshorylated tryptic peptide of beta-casein and Michael addition of the FAT-label.

FIG. 2 illustrates a tandem mass spectrum of the FAT-labeled beta-casein tryptic peptide (SEQ ID NO: 1) acquired by a hybrid-TOF instrument (QSTAR) equipped with an oMALDI source. Asterisk (*) denotes FAT fragment ions which could be used as diagnostic ions for precursor ion scanning.

FIG. 3 shows a tandem mass spectrum of the FAT-labeled beta-casein tryptic peptide (SEQ ID NO: 1) acquired by a hybrid-TOF instrument (QSTAR) equipped with a Protana nano-ESI (electrospray ionization) source. Tandem mass spectrum of the same peptide (triply charged) acquired by a hybrid-TOF instrument equipped with the Protana nano-ESI source. The mass spectrometry/mass spectrometry (MS/MS) spectrum was searched against the nr database (NCBI) using MASCOT. A custom differential modification of serine or threonine corresponding to FAT-label addition was employed in the search (right).

FIG. 4 presents fluorescence images generated from the Typhoon 8600 instrument. Images portrayed are (1) intact FAT-labeled phosphoprotein after ID SDS-PAGE separation (left) and (2) a MALDI plate spotted with varying concentrations of the FAT reagent (right).

FIG. 5 provides mass spectra of FAT-labeled beta casein that was digested in-gel with Lys-C, loaded onto a C18 ZipTip, and fractionated with varying concentrations of acetonitrile onto a MALDI plate. In conjunction with fluorescence imaging, this technique allows for selective targeting of FAT-labeled peptides after fractionation of complex mixtures.

FIG. 6 depicts MALDI-TOF mass spectrum of 500 fmol myoglobin digest spiked with dilute amount of FAT reagent (top trace). The bottom trace is the same digest after affinity purification with an anti-rhodamine affinity microcolumn.

FIG. 7 illustrates a mass spectrum showing the enrichment of FAT-labeled peptides after affinity purification of the beta casein Lys-C digest.

FIG. 8 presents a search of the MS/MS spectrum of the FAT-labeled HPLC-purified tryptic peptide against the nr database (NCBI) using MASCOT. A custom differential modification of serine or threonine corresponding to FAT-label addition was employed in the search.

FIG. 9 is a work flow diagram showing the experimental procedures used to determine extent of cysteine modification as well as the selective enrichment of cysteine-modified peptides.

FIGS. 10A and 10B are isotope coded affinity tags (ICAT) pairs demonstrating variations in acrylamide incorporation. FIG. 10A corresponds to the peptide GLVLIAFSQYLQQC*PFDEHVK which shows more than a 3 fold decrease in mass spectral intensity after treatment of the protein with acrylamide. FIG. 10B displays a peptide (LFTFHADIC*TLPDTEK) with minimal change after treatment of the protein with acrylamide.

FIG. 11 is a table showing quantitation of ICAT pairs from bovine serum albumin (BSA) after QSTAR analysis. Results were exported directly from the ProICAT software. Calculated ratios are indicative of acrylamide incorporation.

FIG. 12A shows the high pressure liquid chromatography ESI mass spectroscopy/mass spectroscopy analysis of the flowthrough obtained from the ICAT affinity purification procedure. FIG. 12B is a MS/MS spectrum validating the acrylamide modification of the cysteine-containing peptide GLVLIAFSQYLQQC*PFDEHVK.

FIG. 13A shows MALDI-TOF mass spectrum of the acrylamide-adducted peptide WHWRPWTPC*KMF. FIG. 13B shows MALDI-TOF mass spectrum of the derivatized peptide after beta-elimination and Michael addition with the fluorescent affinity tag.

FIG. 14 shows HPLC profiles of the fluorescent affinity tag (FAT, black trace) and FAT-labeled peptides (blue traces). Chromatograms were obtained by monitoring absorbance at 520 nm.

DETAILED DESCRIPTION OF THE INVENTION

The present invention pertains to methods and compositions suitable for facilitating the analysis, identification, or purification of thiol-reactive molecules. In one embodiment, the invention relates to analysis, identification, or purification of phosphoproteins. Phosphoproteins or fragments thereof may often be present in small amounts as part of complex mixtures. Incorporation of a fluorescent affinity tag at phosphorylated residues permits both enhanced detection and facile purification with minimal sample manipulation.

Another embodiment of the subject invention provides for the labeling, identification, or purification of nucleic acids or polynucleotides containing phosphate groups (e.g., nucleotide mono-, di-, or triphosphates or polynucleotides containing phosphate groups). In various embodiments, the tags provided herein can be used in methods of detecting nucleic acid interactions (e.g., hybridization). Thus, the subject invention also provides labeled nucleic acid or polynucleotide sequences that are useful in methods such as enzymatic gene amplification (or PCR), Southern blots, Northern blots, or other techniques utilizing hybridization for the identification of polynucleotide sequences in a sample.

In another embodiment, the invention relates the preparation of target-associative tags containing a thiol moiety. Many fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties can be usefully employed in a variety of scenarios dependent on covalent attachment of said discriminating moieties to a reactive thiol capable of acting as a targeting moiety. The reaction of cysteamine or cysteamine-derivatives with said discriminating moieties provides a useful way of preparing such target-associative tags.

In preferred embodiments, the tags of the instant invention have a cysteamine moiety directly attached to discriminating moieties such as fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties; in such embodiments, linkers, such as maleimides are not used to couple the cysteamine moieties to fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties. In other embodiments of the subject invention, the fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties are not thiol reactive (i.e., these moieties attached to a cysteamine or cysteamine-containing element are not attached via the sulfur atom of the cysteamine). Non-limiting examples of fluorescent moieties that can be attached to a cysteamine moiety include rhodamine, fluorescein, coumarin, eosin, erythrosin, lucifier yellow, malachite green, or oregon green.

The subject invention further provides an exemplary fluorescent affinity tag (FAT), or composition thereof, of the formula:

This exemplary FAT, or composition thereof, comprises rhodamine conjugated to a cysteamine moiety.

Compositions comprising the FAT of the subject invention comprise a carrier and at least one FAT. Such compositions may be formulated in any carriers, including for example, carriers described in E. W. Martin's Remington's Pharmaceutical Science, Mack Publishing Company, Easton, Pa. Non-limiting examples of suitable carriers include saline, phosphate buffered saline (PBS), HEPES, TRIS-based buffers, HANKS, or Ringer's solutions.

EXAMPLE 1 Purification of Affinity Tag

A microaffinity column was prepared as follows. Two microliters of Poros Protein G (Applied Biosystems) slurry was incubated with 10 μL of 1 μg/μL anti-rhodamine antibody (Abcam) solution in PBS for 1 hr at 4° C. A gel-loader tip was crimped, packed with the Protein G slurry, and washed three times with PBS.

A 500 fmol myoglobin digest was prepared and spiked with a dilute amount of the FAT reagent. It was not expected that the FAT reagent would react with the peptides of the myoglobin digest because conditions for beta-elimination and Michael addition were not employed. A mass spectrum was taken of the mixture and is presented in FIG. 6 (top trace). The expected profile for the FAT reagent is not prevalent in this mass spectrum due to the relatively more abundant myoglobin-derived species.

The FAT-reagent-containing myoglobin digest was then passed through the microaffinity column several times to ensure maximum binding of the FAT reagent. The column was washed several times with 10 μL PBS to remove nonspecifically bound myoglobin-derived species. After 3×10 μL washes of water to remove excess salt, the affinity-purified FAT reagent was eluted from the column with 2 μL of 2% TFA directly onto a MALDI plate. A mass spectrum was taken of the affinity-purified elution fraction and is presented in FIG. 6 (bottom trace). Peaks attributable to the FAT reagent are now seen to be prevalent, thus indicating a substantial degree of purification of the FAT reagent.

EXAMPLE 2 Analysis by Mass Spectroscopy of FAT-Labeled HPLC-Purified Tryptic Phosphopeptide of Beat-Casein

A sample of beta-casein protein was digested with trypsin and the monophosphorylated peptide FQSEEQQQTEDELQDK (SEQ ID NO: 1) was purified by HPLC. The purified tryptic peptide was subjected to conditions appropriate for beta-elimination of phosphate as described in Knight, et al.; Nat. Biotech., 2003, 21, 1047-1054. After incubation for 1-2 hours at room temperature, Michael addition of the FAT reagent was carried out for an additional 3-6 hours at room temperature.

FIG. 1 presents a mass spectrum used for general screening of reaction progress for the beta-elimination/Michael addition reactions. Ions associated with the partially derivatized peptide (i.e. after beta elimination) are present at a relatively low abundance, while ions associated with the fully derivatized peptide (i.e. after Michael addition of the FAT label) are much more prevalent.

The derivatized peptide was subsequently analyzed by tandem mass spectroscopy. FIG. 2 illustrates a mass spectrum of the FAT-labeled peptide as acquired by a hybrid-TOF instrument (QSTAR) equipped with an oMALDI source. Examples of FAT fragment ions that could be used as diagnostic ions for precursor ion scanning are indicated. FIG. 3 depicts a mass spectrum of the same FAT-labeled peptide as acquired by a hybrid-TOF instrument (QSTAR) equipped with a Protana nano-ESI source. The MS/MS spectrum was searched against the nr database (NCBI) using MASCOT. A custom differential modification of serine or threonine corresponding to FAT-label addition was employed in the search. The search correctly identified the FAT-labeled peptide (FQSEEQQQTEDELQDK) (SEQ ID NO: 1) and the source (beta-casein).

EXAMPLE 3 In-Gel Fluorescence Detection and Proteolytic Digestion Followed by Affinity Purification and Analysis by Mass Spectroscopy

A sample of beta-casein protein was subjected to conditions appropriate for beta-elimination of phosphate. After incubation for 1-2 hours at room temperature, Michael addition of the FAT reagent was carried out for an additional 3-6 hours at room temperature.

Following labeling of the beta casein protein, the protein mixture was separated by 1D SDS-PAGE and the gel was analyzed by a Typhoon 8600 variable mode imager (Amersham Pharmacia Biotech) to map the presence of FAT-labeled phosphoproteins present in the sample. FIG. 4 shows an example of an SDS-PAGE gel containing FAT-labeled beta-casein as imaged by the Typhoon 8600 instrument. Also illustrated is a MALDI plate spotted with different quantities of the FAT reagent alone and imaged by the Typhoon 8600 instrument to demonstrate the sensitivity of the technique to small quantities of FAT label.

Bands that produced a fluorescent signal were digested in-gel with Lys-C (Roche Applied Science). Following the digestion procedure, the digested bands were (1) purified with either a C18 ZipTip or an anti-rhodamine microaffinity column and (2) analyzed by a quadrupole time-of-flight instrument (QSTAR, Applied Biosystems) operated with either MALDI or nano-ESI ionization sources. General screening of reaction progress was performed by a MALDI-TOF instrument (Voyager DE-Pro, Applied Biosystems).

For digested bands purified by ZipTip, FIG. 5 shows mass spectra obtained for ZipTip elution fractions obtained at varying concentrations of acetonitrile. A Typhoon 8600 image overlaid on the figure shows that the fraction eluted with 20% acetonitrile is more highly fluorescent than the fraction eluted with 5% acetonitrile. The corresponding mass spectra show that the more highly fluorescent fraction contains a greater concentration of derivatized (FAT labeled) peptide. Together these data provide an example of the utility of the FAT label for selective fluorescence-based targeting of FAT-labeled (formerly phosphorylated) peptides after fractionation of complex mixtures.

For digested bands purified by affinity chromatography, an anti-rhodamine microaffinity column was prepared as noted previously. The peptide mixture from the digested gel band was dispensed through the microaffinity column several times to ensure maximum binding. The column was washed several times with 10 μL PBS to remove nonspecifically bound peptides. After 3×10 μL washes of water to remove excess salt, FAT-labeled peptides were eluted from the column with 2 μL of 2% TFA directly onto a MALDI plate. FIG. 7 shows the MALDI-TOF mass spectrum in which the affinity enrichment of FAT-labeled peptide is apparent. This provides an example of the utility of the FAT label for selective affinity-based purification of FAT-labeled (formerly phosphorylated) peptides.

EXAMPLE 4 Synthesis of N^(A)[Tetramethylrhodamine 5(6)-Carboxamide]-Arginyl-Cysteamine

N^(α)Fmoc-Arg(Pbf)-OH was coupled to cysteamine-2-chlorotrityl resin (Novobiochem) with dicyclohexycarbodiamide in the presence of 1-hydroxybenzotriazole. The protecting group was removed by 20% piperidine in dimethylforamide (DMF) and then subsequently coupled with 5(6)-carboxytetramethylrhodamine N-hydroxysuccinimide ester in the presence of 1-hydroxybenzotriazole in DMF. The peptide resin was washed with DMF, dichloromethane, methyl alcohol, dichloromethane, ether, and then dried. The peptide was then cleaved from the resin with trifluoroacetic acid (TFA) containing 5% triisopropylsilane and 5% water at room temperature for 1 hour. The resin/TFA mixture was filtered into cooled tert-butyl methyl ether. The precipitated peptide was separated by centrifugation and washed three times with fresh tert-butyl methyl ether. The peptide derivatives were then purified by reversed phase (C18) HPLC.

Example 5 Manufacture and Analysis of Acrylamide Modified Peptides

Numerous mass spectrometric-based quantitation methods have been developed for profiling variations in protein expression. Commercially available Isotope Coded Affinity Tags (ICAT) have been commonly utilized for this purpose yet the selectivity of this method for cysteine-containing peptides has stimulated concern about protein coverage and the quantitation of posttranslational modifications. ICAT selectivity, however, is ideal for the analysis of cysteine-targeted chemical or posttranslational modifications. In addition to implementing this technology, we have developed a novel approach for the direct analysis of modified cysteine residues that involves beta-elimination/Michael addition chemistries using a fluorescent affinity tag.

Acrylamide is capable of forming adducts with free thiol groups on proteins and we have shown that these acrylamide modifications occur on multiple cysteine residues of bovine serum albumin using ESI-qTOF-MS and MS/MS. By labeling the control and acrylamide-treated protein samples with the “light (13C-0)” and “heavy (13C-9)” form of the ICAT reagent, respectively, the amount of acrylamide incorporation was measured by the decrease in mass spectral intensity of the 13C-9 labeled peptide. Since acrylamide-modified cysteines are inert to the ICAT-labeling process, peptides containing this modification were present in the flow-through obtained after avidin affinity separation.

The flow-through was subjected to beta-elimination conditions and allowed to react with the FAT-label via Michael addition chemistry. FAT-labeled peptide standards and BSA-derived peptides were successfully identified and characterized by HPLC separation (monitoring a label-specific wavelength of 520 nm) and mass spectrometry. Quantitation of acrylamide reactivity with bovine serum albumin and the enhanced detection of acrylamide-modified cysteine residues have been demonstrated using this methodology.

ICAT-labeling experiments were performed according to the manufacturer's (Applied Biosystems, Foster City, Calif.) instructions. Following the ICAT affinity purification procedure, the flow-through and wash samples were saved for subsequent beta-elimination and Michael addition derivatization of the modified cysteine residues. Quantification of cysteine modification by acrylamide was accomplished by the ProICAT software package (Applied Biosystems, Foster City, Calif.). Beta-elimination of acrylamide-modified cysteine residues was carried out at 37° C for 1 hour followed by Michael addition of the fluorescent affinity tag (rhodamine-containing label) for an additional 2 hours. Derivatized cysteine-containing peptides were purified and fractionated by reversed-phase HPLC monitored at 520 nm (rhodamine-specific absorption). Mass spectrometric analysis was performed on a hybrid quadrupole, time-of-flight instrument (QSTAR, Applied Biosystems) or a MALDI-TOF (Voyager DE-PRO, Applied Biosystems) mass spectrometer.

After ICAT labelling of the control and acrylamide treated BSA samples, the corresponding tryptic peptides were analyzed by HPLC-ESI-MS/MS via the QSTAR instrument. Two representative ICAT pairs are displayed demonstrating variations in acrylamide incorporation. The top mass spectrum of FIG. 10 (FIG. 10A) corresponds to the peptide GLVLIAFSQYLQQC*PFDEHVK which shows more than a 3 fold decrease in mass spectral intensity after treatment of the protein with acrylamide. The bottom mass spectrum (FIG. 10B) displays a peptide (LFTFHADIC*TLPDTEK)with minimal change after treatment of the protein with acrylamide. FIG. 11 provides a quantitation of ICAT pairs from BSA after QSTAR analysis. Results were exported directly from the ProICAT software. Calculated ratios are indicative of acrylamide incorporation. In FIG. 12A, HPLC-ESI-MS/MS analysis of the flowthrough obtained from the ICAT affinity purification procedure is illustrated. The bottom figure (FIG. 12B) is a MS/MS spectrum validating the acrylamide modification of the cysteine-containing peptide GLVLIAFSQYLQQC*PFDEHVK. FIG. 13A provides MALDI-TOF mass spectrum of the acrylamide-adducted peptide WHWRPWTPC*KMF. FIG. 13B illustrates MALDI-TOF mass spectrum of the derivatized peptide after beta-elimination and Michael addition with the fluorescent affinity tag. Finally, FIG. 14 provides HPLC profiles of the fluorescent affinity tag (FAT, black trace) and FAT-labelled peptides (blue traces). Chromatograms were obtained by monitoring absorbance at 520 nm. 

1-24. (canceled)
 25. A composition of matter comprising: a) an isolated compound of the formula:

b) an isolated compound comprising a cysteamine moiety directly attached to a discriminating moiety selected from fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties; c) an isolated compound comprising a cysteamine moiety directly attached to a discriminating moiety selected from rhodamine, fluorescein, coumarin, eosin, erythrosin, lucifier yellow, malachite green, or oregon green; d) a composition comprising a carrier and a compound comprising a cysteamine moiety directly attached to a discriminating moiety selected from fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties; e) a composition comprising a carrier and a compound directly attached to a discriminating moiety selected from fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties, wherein said compound is

f) a nucleotide, nucleic acid, polynucleotide, amino acid, protein, peptide, or polypeptide attached, via a phosphate group, to a compound of the formula:

g) a nucleotide, nucleic acid, polynucleotide, amino acid, protein, peptide, or polypeptide attached, via a phosphate group, to a compound comprising a cysteamine moiety directly attached to a discriminating moiety selected from fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties; h) a nucleotide, nucleic acid, polynucleotide, amino acid, protein, peptide, or polypeptide attached, via a phosphate group, to a compound comprising a cysteamine moiety directly attached to a discriminating moiety selected from rhodamine, fluorescein, coumarin, eosin, erythrosin, lucifier yellow, malachite green, or oregon green; i) a composition comprising a carrier and a nucleotide, nucleic acid, polynucleotide, amino acid, protein, peptide, or polypeptide attached, via a phosphate group, to a compound comprising a cysteamine moiety directly attached to a discriminating moiety selected from fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties; or j) a composition comprising a carrier and a nucleotide, nucleic acid, polynucleotide, amino acid, protein, peptide, or polypeptide attached, via a phosphate group, to a compound directly attached to a discriminating moiety selected from fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties, wherein said compound is


26. A method of labeling a phosphate containing nucleotide, nucleic acid, polynucleotide, amino acid, protein, peptide, or polypeptide comprising contacting a phosphate containing nucleotide, nucleic acid, polynucleotide, protein, peptide, or polypeptide with a tag comprising both (1) a fluorophore, chromophore, magnetic particle, gold particle, isotopic mass label, or other discriminating moiety and (2) a moiety suitable for affinity binding under conditions that allow for the incorporation of said tag into said nucleotide, nucleic acid, polynucleotide, amino acid, protein, peptide, or polypeptide at a phosphate group.
 27. The method of claim 26, wherein said tag provides for at least one or both of the following: (1) detecting said labeled phosphate containing nucleotide, nucleic acid, polynucleotide, amino acid, protein, peptide, or polypeptide by fluorescence; or (2) isolating said phosphate containing nucleotide, nucleic acid, polynucleotide, protein, peptide, or polypeptide by an affinity interaction.
 28. The method according to claim 26, wherein said tag has the formula:


29. The method according to claim 26, wherein said moiety is cysteamine.
 30. The method according to claim 26, wherein said tag replaces at least one phosphate group in said phosphate containing nucleotide, nucleic acid, polynucleotide, amino acid, protein, peptide, or polypeptide.
 31. A method of attaching a molecule to a phosphate containing (phosphorylated) nucleotide, nucleic acid, amino acid, protein, peptide, or polypeptide comprising reacting a molecule with cysteamine or with a cysteamine-containing compound to give derivatized cysteamine and reacting said derivatized cysteamine with said phosphate containing nucleotide, nucleic acid, polynucleotide, amino acid, protein, peptide, or polypeptide.
 32. The method of claim 31, wherein said molecule comprises a fluorophore.
 33. The method of claim 31, wherein said molecule comprises a moiety suitable for affinity binding.
 34. The method of claim 31, wherein said reacting of said derivatized cysteamine with said protein results in the formation of a covalent bond between the cysteaminyl sulfur atom and said protein.
 35. A method of mapping phosphorylation sites in proteins, peptides, or polypeptides comprising replacement of one or more phosphate group in a protein, peptide, or polypeptide with an affinity tag and mapping said phosphorylation sites and performing mass spectroscopy to map said phosphorylation sites.
 36. The method according to claim 35, wherein said affinity tag is a fluorescent affinity tag (FAT).
 37. The method according to claim 36, wherein said fluorescent affinity tag is


38. A method of labeling a phorylated compound comprising contacting a phosphorylated compound with a compound comprising a cysteamine moiety directly attached to a discriminating moiety selected from fluorophores, chromophores, reactive groups, magnetic particles, gold particles, isotopic mass labels, or other discriminating moieties.
 39. The method according to claim 38, wherein said phosphorylated compound is a nucleotide, nucleic acid, polynucleotide, amino acid, polypeptide, peptide or protein.
 40. The method according to claim 28, further comprising the purification of said labeled compound.
 41. The method according to claim 39, further comprising the purification of said labeled compound. 